Department of Abdominal and Pelvic Surgery, INCA, Rio de Janeiro, Brazil.
Instituto COI de Educação e Pesquisa, Rio de Janeiro, Brazil.
Support Care Cancer. 2022 Aug;30(8):6557-6572. doi: 10.1007/s00520-022-07059-6. Epub 2022 Apr 29.
Neoadjuvant chemoradiotherapy (neoCRT) followed by surgery is the standard of care for locally advanced rectal cancer (LARC), but the emergence of different drug regimens may result in different response rates. Good clinical response translates into greater sphincter preservation, but quality of life (QOL) may be impaired after treatment due to chemoradiotherapy and surgical side effects.
To prospectively evaluate the impact of clinical response and surgical resection on QOL in a randomized trial comparing two different neoCRT regimens.
Stage II and III rectal cancer patients were randomized to receive neoCRT with either capecitabine (group 1) or 5-Fu and leucovorin (group 2) concomitant to long-course radiotherapy. Clinical downstaging was accessed using MRI 6-8 weeks after treatment. EORTCs QLQ-C30 and CR38 were applied before treatment (T0), after neoCRT (T1), after rectal resection (T2), early after adjuvant chemotherapy (T3), and 1 year after the end of treatment or stoma closure (T4). The Wexner scale was used for fecal incontinence evaluation at T4. A C30SummaryScore (Geisinger and cols.) was calculated to compare QOL results.
Thirty-two patients were assigned to group 1 and 31 to group 2. Clinical downstaging occurred in 70.0% of group 1 and 53.3% of group 2 (p = 0.288), and sphincter preservation was 83.3% in group 1 and 80.0% in group 2 (p = 0.111). No significant difference in QOL was detected when comparing the two treatment groups after neoCRT using QLQ-C30. However, the CR38 module detected differences in micturition problems (15.3 points), gastrointestinal problems (15.3 points), defecation problems (11.8 points), and sexual satisfaction (13.3 points) favoring the capecitabine group. C30SummaryScore detected significant improvement comparing T0 to T1 and deterioration comparing T1 to T2 (p = 0.025). The mean Wexner scale score was 9.2, and a high score correlated with symptoms of diarrhea and defecation problems at T4.
QOL was equivalent between groups after neoCRT except for micturition problems, gastrointestinal problems, defecation problems, and sexual satisfaction favoring the capecitabine arm after. The overall QOL using the C30SummaryScore was improved after neoCRT, but decreased following rectal resection, returning to basal levels at late evaluation. Fecal incontinence was high after sphincter preservation.
ClinicalTrials.gov Identifier: NCT03428529.
新辅助放化疗(neoCRT)后手术是局部晚期直肠癌(LARC)的标准治疗方法,但不同药物方案的出现可能导致不同的缓解率。良好的临床缓解意味着更大的肛门保留,但由于放化疗和手术的副作用,治疗后生活质量(QOL)可能会受到损害。
前瞻性评估两种不同 neoCRT 方案的临床缓解和手术切除对 QOL 的影响。
II 期和 III 期直肠癌患者随机接受 neoCRT,分别接受卡培他滨(第 1 组)或 5-Fu 和亚叶酸(第 2 组)联合长程放疗。治疗后 6-8 周采用 MRI 评估临床降期。EORTCs QLQ-C30 和 CR38 在治疗前(T0)、neoCRT 后(T1)、直肠切除后(T2)、辅助化疗早期(T3)和治疗结束后 1 年或造口关闭后(T4)进行评估。T4 时使用 Wexner 量表评估粪便失禁。计算 C30SummaryScore(Geisinger 等人)以比较 QOL 结果。
32 例患者被分配到第 1 组,31 例患者被分配到第 2 组。第 1 组的临床降期率为 70.0%,第 2 组为 53.3%(p=0.288),第 1 组的肛门保留率为 83.3%,第 2 组为 80.0%(p=0.111)。使用 QLQ-C30 比较 neoCRT 后两组之间的 QOL 时,未发现明显差异。然而,CR38 模块检测到排尿问题(15.3 分)、胃肠道问题(15.3 分)、排便问题(11.8 分)和性满意度(13.3 分)方面存在差异,卡培他滨组更为有利。C30SummaryScore 检测到 T0 与 T1 比较有显著改善,T1 与 T2 比较有恶化(p=0.025)。平均 Wexner 量表评分为 9.2,高分与 T4 时腹泻和排便问题的症状相关。
除了卡培他滨组的排尿问题、胃肠道问题、排便问题和性满意度外,两组在 neoCRT 后 QOL 相当。使用 C30SummaryScore 的整体 QOL 在 neoCRT 后得到改善,但直肠切除后下降,在晚期评估时恢复到基础水平。括约肌保留后的粪便失禁率较高。
ClinicalTrials.gov 标识符:NCT03428529。